Canonical Allele Identifier: CA563498506

Gene: SLC23A1

Linked Data

• dbSNP Id: rs1268276412
• gnomAD v2: 5-138715326-G-A
• MyVariant Identifiers: chr5:g.138715326G>A (hg19) ; chr5:g.139379637G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.139379637G>A , CM000667.2:g.139379637G>A	GRCh38
NC_000005.9:g.138715326G>A , CM000667.1:g.138715326G>A	GRCh37
NC_000005.8:g.138743225G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348729.8:c.925+41C>T MANE Select	ENSP00000302701.4:n.925+41C>T
ENST00000348729.7:c.925+41C>T	ENSP00000302701.4:n.925+41C>T
ENST00000353963.7:c.937+41C>T	ENSP00000302851.5:n.937+41C>T
ENST00000504513.1:c.165-283C>T
ENST00000506512.1:n.536+41C>T
NM_005847.4:c.925+41C>T	NP_005838.3:n.925+41C>T
NM_152685.3:c.937+41C>T	NP_689898.2:n.937+41C>T
XM_005272148.3:c.1045+41C>T	XP_005272205.3:n.1045+41C>T
XM_005272149.3:c.1033+41C>T	XP_005272206.3:n.1033+41C>T
XM_006714741.2:c.1045+41C>T	XP_006714804.2:n.1045+41C>T
XM_011543765.1:c.1045+41C>T	XP_011542067.1:n.1045+41C>T
XM_011543766.1:c.826+41C>T	XP_011542068.1:n.826+41C>T
XM_011543767.1:c.730+41C>T	XP_011542069.1:n.730+41C>T
XM_011543768.1:c.610+41C>T	XP_011542070.1:n.610+41C>T
XM_011543769.1:c.220+41C>T	XP_011542071.1:n.220+41C>T
XM_005272149.4:c.1033+41C>T	XP_005272206.3:n.1033+41C>T
XM_011543765.2:c.1045+41C>T	XP_011542067.1:n.1045+41C>T
NM_005847.5:c.925+41C>T MANE Select	NP_005838.3:n.925+41C>T
NM_152685.4:c.937+41C>T	NP_689898.2:n.937+41C>T